Curtis A, Millan F, Holloway S, Mennie M, Crosbie A, Raeburn J A, Brock D J
Human Genetics Unit, University of Edinburgh, Western General Hospital, UK.
Hum Genet. 1989 Jan;81(2):188-90. doi: 10.1007/BF00293901.
Presymptomatic testing for Huntington's disease (HD) is possible through the use of restriction fragment length polymorphisms (RFLPs) at the closely linked D4S10 locus. Recombination between the HD and D4S10 loci will occur in 4%-5% of meioses, and is a well-recognised complication of predictive testing. Recombination between RFLPs within the D4S10 locus is a rare event and can usually be ignored. We report a case where such an intra-locus recombination frustrated attempts to predict the chance of a high-risk individual inheriting the HD gene.
通过使用紧密连锁的D4S10位点的限制性片段长度多态性(RFLP),可以对亨廷顿舞蹈病(HD)进行症状前检测。HD和D4S10位点之间的重组将在4%-5%的减数分裂中发生,这是预测性检测中一个公认的复杂情况。D4S10位点内RFLP之间的重组是一个罕见事件,通常可以忽略不计。我们报告了一个病例,其中这种位点内重组阻碍了预测高危个体遗传HD基因几率的尝试。